79 top medical experts on Type 1C Charcot-Marie-Tooth disease across 7 countries and 1 U.S. states, including 3 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Type 1C Charcot-Marie-Tooth disease: A rare, autosomal dominant, hereditary, demyelinating motor and sensory neuropathy which may present either as a classic Charcot-Marie-Tooth disease phenotype with distal motor weakness and wasting, gait difficulties, parethesias, decreased vibration and pain sensation, or as a milder, predominantly sensory form with transient paresthesias, decreased sensation and distal pain in upper or lower limbs, without significant motor weakness. Pes cavus is a common feature, and additional symptoms may include hand tremor and decreased or absent deep tendon reflexes.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Slow Nerve Conduction Type C CMT,  CMT1C,  Type IC Hereditary Motor And Sensory Type 1C Neuropathy Charcot-Marie-Tooth Neuropathy,  Type 1C demyelinating Charcot-Marie-Tooth disease,  HMSN1C,  HMSNIC


  

        

                    


    Computing Expert Listing ...